{{Rsnum
|rsid=12638862
|Chromosome=3
|position=169759718
|Orientation=plus
|GMAF=0.3306
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 53.1 | 39.8 | 7.1
| HCB | 14.6 | 55.5 | 29.9
| JPT | 7.1 | 48.7 | 44.2
| YRI | 81.0 | 18.4 | 0.7
| ASW | 71.9 | 24.6 | 3.5
| CHB | 14.6 | 55.5 | 29.9
| CHD | 23.9 | 45.0 | 31.2
| GIH | 59.4 | 34.7 | 5.9
| LWK | 67.3 | 30.0 | 2.7
| MEX | 36.2 | 53.4 | 10.3
| MKK | 71.2 | 24.4 | 4.5
| TSI | 61.8 | 33.3 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (IgH translocation)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=A
  |Pval=2E-6
  |OR=1.37
  |ORtxt=[1.20-1.56]
  }}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}